Evidence map›Paper›PMID 38991365›Full record

ArticleInternational journal of surgery case reports2024

Rare case of giant ischiorectal leiomyosarcoma.

Kalkidan Kibret Mekoya, Sherefa Hussein Sula, Kaleab Habtemichael Gebreselassie, Kalid Sherefa Reshid

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In one paragraph

Article in International journal of surgery case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kalkidan Kibret MekoyaWerabe university and Werabe Comprehensive Specialized Hospital, Department of Surgery, Werabe, Ethiopia. Electronic address: kalkibret3@gmail.com.
Sherefa Hussein SulaDepartment of Surgery, Werabe Comprehensive Specialized Hospital, Werabe, Ethiopia.
Kaleab Habtemichael GebreselassieDepartment of Surgery, Urology Unit, Werabe Comprehensive Specialized Hospital, Werabe, Ethiopia.
Kalid Sherefa ReshidDepartment of Surgery, Werabe Comprehensive Specialized Hospital, Werabe, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLeiomyosarcoma is a rare type of soft tissue sarcoma especially giant ones (size >5 cm). It is usually arises from the uterus and retroperitoneum. Ischiorectal space is not a common site for primary leomyosarcoma. There are only few case reports about Ischiorectal leiomyosarcoma. PRESENTATION OF CASE: We present a case of 25 yrs. old female patient, who presented with a swelling on left buttock. It measures 9 by 9.5 by 18 cm on MRI. Complete tumor excision done and immunohistochemistry tests confirmed the diagnosis of leiomyosarcoma. DISCUSSION: Due to its rarity, unusual site and large size leiomyosarcoma poses a great challenge for a surgeon both to diagnose and manage it. Early diagnosis and management improves prognosis and decreases recurrence rate because sarcomas have high recurrence rate. It is highly recommended to have multidisciplinary approach.

conclusionThe case report highlights on both diagnostic and therapeutic challenges associated with giant leiomyosarcoma. There are no strict guidelines to follow when managing this type of cases but rather approach has to be individualized. Since there are only few case reports on this specific pathology we advocate for surgeons to share their experience on similar cases.

Indexed as

Gaint leiomyosarcomaIschiorectal spaceLeiomyosarcoma

Identifiers

PMID38991365
PMCPMC11295951

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.